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MONOJECT ARTERIAL BLOOD SAMPLING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K790196
510(k) Type
Traditional
Applicant
SHERWOOD MEDICAL INDUSTRIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1979
Days to Decision
47 days

MONOJECT ARTERIAL BLOOD SAMPLING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K790196
510(k) Type
Traditional
Applicant
SHERWOOD MEDICAL INDUSTRIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1979
Days to Decision
47 days